Oral delivery of miR-146a-5p overexpression plasmid-loaded Pickering double emulsion modulates intestinal inflammation and the gut microbe

罗伊乳杆菌 炎症 细胞生物学 肠粘膜 小RNA 下调和上调 化学 微生物学 生物 益生菌 免疫学 细菌 生物化学 医学 基因 内科学 遗传学
作者
Jiahao Zhu,Yaotian Fan,Songfeng Yang,Mengran Qin,Xingping Chen,Junyi Luo,Ting Chen,Jiajie Sun,Yongliang Zhang,Qianyun Xi
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:261 (Pt 2): 129733-129733 被引量:7
标识
DOI:10.1016/j.ijbiomac.2024.129733
摘要

The function of miRNAs in intestinal inflammatory injury regulation has been studied extensively. However, the targeted delivery of these functional nucleic acid molecules to specific organs through encapsulation carriers and exerting their functional effects remain critical challenges for further research. Here, we constructed miR-146a-5p overexpression plasmid and validated the anti-inflammatory properties in the cell model. Then, the plasmid was encapsulated by the Pickering double emulsion system to investigate the role of Pickering double emulsion system in LPS-induced acute intestinal inflammatory injury. The results showed that the Pickering double emulsion system could effectively protect the integrity of plasmids in the intestinal tract, alleviate intestinal inflammatory injury, and upregulate the relative abundance of Lactobacillus reuteri. Mechanically, in vivo and in vitro experiments have shown that miR-146a-5p inhibits TLR4/NF-κB pathway to alleviate intestinal inflammation. In addition, miR-146a-5p can also regulate intestinal homeostasis by targeting the RNA polymerase sigma factor RpoD and α-galactosidase A, thereby affecting the growth of Lactobacillus reuteri. Above all, this study reveals a potential mechanism for miR-146a-5p to treat intestinal inflammation and provides a new delivery strategy for miRNAs to regulate intestinal homeostasis.
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